Allele Registry

Canonical Allele Identifier: PA916011500

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491737

ClinVar Variation:

428424

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu989Lys	CA346758765 NM_001281492.2:c.2965G>A