Canonical Allele Identifier: PA645447837
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 246632
ClinVar RCV Id: RCV001015419 RCV001764220 RCV002229376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Gly801Arg
CA10584664
NM_001127500.3:c.2401G>C
CA368982493
NM_001127500.3:c.2401G>A