Allele Registry

Canonical Allele Identifier: PA2826625815

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000792081

RCV002386376

ClinVar Variation:

639316

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly330Asp	CA346744976 NM_001281492.2:c.989G>A