Allele Registry

Canonical Allele Identifier: PA2573200944

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002012246

ClinVar Variation:

1448825

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Tyr800Asp	CA368991595 NM_001324402.2:c.2398T>G