Allele Registry

Canonical Allele Identifier: PA916012191

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216969

RCV000684809

RCV000767045

RCV003460689

RCV004017385

ClinVar Variation:

89449

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg940Ser	CA014030 NM_001281494.2:c.2818C>A