Allele Registry

Canonical Allele Identifier: PA1139672193

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001181922

RCV001217719

RCV004006767

ClinVar Variation:

922073

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln236Lys	CA346739980 NM_000179.3:c.706C>A