Allele Registry

Canonical Allele Identifier: PA2826630163

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000792081

RCV002386376

ClinVar Variation:

639316

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gly158Asp	CA346744976 NM_001281493.2:c.473G>A