Allele Registry

Canonical Allele Identifier: PA2826625704

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000485339

RCV001312494

RCV002380619

RCV002381687

RCV003454502

ClinVar Variation:

216294

1769181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe302Leu	CA337394 NM_001281492.2:c.906T>G CA346744219 NM_001281492.2:c.904T>C CA346744228 NM_001281492.2:c.906T>A