Allele Registry

Canonical Allele Identifier: PA2826635156

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001012805

ClinVar Variation:

819882

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly269Ser	CA346748571 NM_001281494.2:c.805G>A