MYL2 c.52T>A ;(p.F18I)

Variant ID: 12-111356949-A-T

NM_000432.3(MYL2):c.52T>A;(p.F18I)

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:

NECTAR: a database of codon-centric missense variant annotations.

Nucleic Acids Research
Gong, Sungsam S; Ware, James S JS; Walsh, Roddy R; Cook, Stuart A SA
Publication Date: 2014-01

Variant appearance in text: MYL2: 52T>A
PubMed Link: 24297257
Variant Present in the following documents:
  • Main text
  • gkt1245.pdf
View BVdb publication page