Allele Registry

Canonical Allele Identifier: PA093713

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000437499

ClinVar Variation:

376728

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Asp1228His	CA16603136 NM_000245.4:c.3682G>C