Canonical Allele Identifier: PA2825103642
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411903
ClinVar RCV Id: RCV002230652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Pro978Leu
CA16612265
NM_000245.4:c.2933C>T