Allele Registry

Canonical Allele Identifier: PA241166

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000175410

RCV000417458

RCV000431224

ClinVar Variation:

194929

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Tyr1248His	CA241164 NM_001127500.3:c.3742T>C