Allele Registry

Canonical Allele Identifier: PA337396

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 216294

ClinVar Variation Id: 1769181

ClinVar RCV Id: RCV002380619

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe432Leu	CA337394 NM_000179.3:c.1296T>G CA346744219 NM_000179.3:c.1294T>C CA346744228 NM_000179.3:c.1296T>A