Allele Registry

Canonical Allele Identifier: PA2825103871

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000418101

ClinVar Variation:

376729

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Asn1100Tyr	CA16603137 NM_000245.4:c.3298A>T