Canonical Allele Identifier: PA123613
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13889
ClinVar RCV Id: RCV000014903 RCV000427546
ClinVar Variation Id: 376201
ClinVar RCV Id: RCV000438241
ClinVar Variation Id: 376202
ClinVar RCV Id: RCV000419338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Met1268Ile
CA123611
NM_001127500.3:c.3804G>A
CA16602656
NM_001127500.3:c.3804G>C
CA16602657
NM_001127500.3:c.3804G>T