Allele Registry

Canonical Allele Identifier: PA2825102920

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002230649

ClinVar Variation:

411892

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Leu605del	CA16612145 NM_000245.4:c.1812_1814del