Allele Registry

Canonical Allele Identifier: PA915963938

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000792081

RCV002386376

ClinVar Variation:

639316

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly460Asp	CA346744976 NM_000179.3:c.1379G>A