Allele Registry

Canonical Allele Identifier: PA645383831

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491737

ClinVar Variation:

428424

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu1119Lys	CA346758765 NM_000179.3:c.3355G>A