Allele Registry

Canonical Allele Identifier: PA2580134046

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002806686

ClinVar Variation:

1994202

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Leu762Phe	CA4448442 NM_001127500.3:c.2284C>T