Allele Registry

Canonical Allele Identifier: PA2573163363

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001982099

RCV003289257

ClinVar Variation:

1432785

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe573Leu	CA346748631 NM_000179.3:c.1717T>C CA346748664 NM_000179.3:c.1719T>A CA346748667 NM_000179.3:c.1719T>G