Allele Registry

Canonical Allele Identifier: PA2826625824

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000777082

RCV003594034

ClinVar Variation:

631046

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro332Ala	CA346745020 NM_001281492.2:c.994C>G