Allele Registry

Canonical Allele Identifier: PA294211

Gene: MSH6 HGNC NCBI

ClinVar Allele:

151588

ClinVar RCV:

RCV000130571

RCV000235178

RCV000475467

RCV001527050

RCV003998064

ClinVar Variation:

141874

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser9Gly	CA010478 NM_000179.3:c.25A>G