Allele Registry

Canonical Allele Identifier: PA2825622245

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002349206

RCV003102432

ClinVar Variation:

1734426

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Asp1246Tyr	CA368991564 NM_001127500.3:c.3736G>T