MED16 c.976T>A ;(p.S326T)

Variant ID: 19-884912-A-T

NM_005481.2(MED16):c.976T>A;(p.S326T)

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: