Allele Registry

Canonical Allele Identifier: PA645383152

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218455

RCV000467310

ClinVar Variation:

232917

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu995Lys	CA10578125 NM_000179.3:c.2983G>A