Canonical Allele Identifier: PA915966744
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 659496
ClinVar RCV Id: RCV000816516 RCV001015393 RCV003442109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Glu799Ala
CA4448456
NM_001127500.3:c.2396A>C