Canonical Allele Identifier: PA167283
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 142059
ClinVar RCV Id: RCV000130870 RCV000199439 RCV000484898 RCV000515234 RCV001262296 RCV001328509 RCV003415953 RCV003320572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Val136Ile
CA167281
NM_001127500.3:c.406G>A