Allele Registry

Canonical Allele Identifier: PA645382860

Gene: MSH6 HGNC NCBI

ClinVar Allele:

392952

ClinVar RCV:

RCV000460082

RCV000580547

RCV003463940

RCV004001849

RCV004525934

ClinVar Variation:

410500

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala940Ser	CA069657 NM_000179.3:c.2818G>T