Canonical Allele Identifier: PA2825103644
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 822441
ClinVar RCV Id: RCV001017804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.His979Tyr
CA368987098
NM_000245.4:c.2935C>T