Allele Registry

Canonical Allele Identifier: PA093792

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000014903

RCV000419338

RCV000427546

RCV000438241

ClinVar Variation:

13889

376201

376202

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Met1250Ile	CA123611 NM_000245.4:c.3750G>A CA16602656 NM_000245.4:c.3750G>C CA16602657 NM_000245.4:c.3750G>T