Allele Registry

Canonical Allele Identifier: PA2825088168

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003078884

ClinVar Variation:

2162051

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu463Lys	CA346745060 NM_000179.3:c.1387G>A