Allele Registry

Canonical Allele Identifier: PA2827253947

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002230649

ClinVar Variation:

411892

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Leu175del	CA16612145 NM_001324402.2:c.522_524del