Allele Registry

Canonical Allele Identifier: PA2826633002

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491737

ClinVar Variation:

428424

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu817Lys	CA346758765 NM_001281493.2:c.2449G>A