Allele Registry

Canonical Allele Identifier: PA093735

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000435140

ClinVar Variation:

376068

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.His1094Tyr	CA16602530 NM_000245.4:c.3280C>T