Allele Registry

Canonical Allele Identifier: PA645382313

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000568833

RCV001297702

RCV003998720

ClinVar Variation:

237161

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asp857Asn	CA069199 NM_000179.3:c.2569G>A