Canonical Allele Identifier: PA2825621252
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 3232964
ClinVar RCV Id: RCV004523596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Pro1009Leu
CA368987272
NM_001127500.3:c.3026C>T