Allele Registry

Canonical Allele Identifier: PA916027408

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002230649

ClinVar Variation:

411892

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311330.1:p.Leu605del	CA16612145 NM_001324401.3:c.1812_1814del