Allele Registry

Canonical Allele Identifier: PA2826626419

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003090265

ClinVar Variation:

2165988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Lys473Glu	CA346749367 NM_001281492.2:c.1417A>G