Allele Registry

Canonical Allele Identifier: PA2826628623

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003461944

ClinVar Variation:

2676808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser1065Gly	CA346760519 NM_001281492.2:c.3193A>G