Allele Registry

Canonical Allele Identifier: PA2826626397

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115383

RCV000233835

RCV000409692

RCV000562745

RCV001800402

RCV003997237

ClinVar Variation:

127564

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe466Ile	CA009191 NM_001281492.2:c.1396T>A