Allele Registry

Canonical Allele Identifier: PA123613

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000014903

RCV000419338

RCV000427546

RCV000438241

ClinVar Variation:

13889

376201

376202

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Met1268Ile	CA123611 NM_001127500.3:c.3804G>A CA16602656 NM_001127500.3:c.3804G>C CA16602657 NM_001127500.3:c.3804G>T