Canonical Allele Identifier: PA2825103246
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2066162
ClinVar RCV Id: RCV002948951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Val776Ile
CA368982378
NM_000245.4:c.2326G>A