Allele Registry

Canonical Allele Identifier: PA2826626347

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160670

RCV000545304

RCV000774598

RCV000781596

RCV003998493

ClinVar Variation:

182625

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Val456Ala	CA009128 NM_001281492.2:c.1367T>C