Canonical Allele Identifier: PA1139677592
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 849997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Asn796Thr
CA368982413
NM_001127500.3:c.2387A>C