Canonical Allele Identifier: PA658669390
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 454204
ClinVar RCV Id: RCV000532305 RCV001013919 RCV000592240 RCV001328521 RCV003153672 RCV003459163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Ser663Leu
CA4448351
NM_001127500.3:c.1988C>T