Allele Registry

Canonical Allele Identifier: PA2826624932

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003176368

ClinVar Variation:

2447295

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser122Leu	CA346740139 NM_001281492.2:c.365C>T