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MYH7 c.962C>T ;(p.A321V)
Variant ID: 14-23899806-G-A
NM_000257.2(
MYH7
):c.962C>T;(p.A321V)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Impact of systolic dysfunction in genotyped hypertrophic cardiomyopathy.
Clinical Cardiology
Fujino, Noboru N; Konno, Tetsuo T; Hayashi, Kenshi K; Hodatsu, Akihiko A; Fujita, Takashi T; Tsuda, Toyonobu T; Nagata, Yoji Y; Kawashiri, Masa-aki MA; Ino, Hidekazu H; Yamagishi, Masakazu M
Publication Date: 2013-03
Variant appearance in text: MYH7: Ala321Val
PubMed Link:
23197398
Variant Present in the following documents:
Main text
View BVdb publication page