Allele Registry

Canonical Allele Identifier: PA2825622311

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001913968

RCV004044041

ClinVar Variation:

1420031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Lys1262Thr	CA368991796 NM_001127500.3:c.3785A>C