CCT5 c.1401C>A ;(p.G467=)

Variant ID: 5-10263329-C-A

NM_012073.3(CCT5):c.1401C>A;(p.G467=)

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: