Allele Registry

Canonical Allele Identifier: PA645448193

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000418101

ClinVar Variation:

376729

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Asn1118Tyr	CA16603137 NM_001127500.3:c.3352A>T