Canonical Allele Identifier: PA645447832
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411912
ClinVar RCV Id: RCV000572470 RCV001293447 RCV001292908 RCV001566122 RCV003470498 RCV003492062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Pro791Leu
CA4448450
NM_001127500.3:c.2372C>T