Allele Registry

Canonical Allele Identifier: PA2825091696

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 823881

ClinVar RCV Id: RCV001020518

ClinVar Variation Id: 1347029

ClinVar RCV Id: RCV002032950

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe1174Leu	CA346760210 NM_000179.3:c.3520T>C CA346760215 NM_000179.3:c.3522T>A CA346760216 NM_000179.3:c.3522T>G