Canonical Allele Identifier: PA093792
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13889
ClinVar Variation Id: 376201
ClinVar RCV Id: RCV000438241
ClinVar Variation Id: 376202
ClinVar RCV Id: RCV000419338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Met1250Ile
CA123611
NM_000245.4:c.3750G>A
CA16602656
NM_000245.4:c.3750G>C
CA16602657
NM_000245.4:c.3750G>T