Canonical Allele Identifier: PA337280
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_001120972.1:p.Val1377Ile
CA337278
NM_001127500.3:c.4129G>A