Canonical Allele Identifier: PA1139677769
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 856076
ClinVar RCV Id: RCV001061469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Thr995Ile
CA368987081
NM_001127500.3:c.2984C>T