Allele Registry

Canonical Allele Identifier: PA2826634136

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160703

RCV000229406

RCV000576090

RCV000663168

RCV000766290

RCV001798555

RCV003462097

RCV003998506

ClinVar Variation:

182650

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ala1045Pro	CA015325 NM_001281493.2:c.3133G>C