Canonical Allele Identifier: PA916027612
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 216510
ClinVar RCV Id: RCV000197534 RCV000569392 RCV001358794 RCV003238734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Val929Ile
CA337278
NM_001324402.2:c.2785G>A