Allele Registry

Canonical Allele Identifier: PA2826624860

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001181922

RCV001217719

RCV004006767

ClinVar Variation:

922073

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln106Lys	CA346739980 NM_001281492.2:c.316C>A