Canonical Allele Identifier: PA2825103237
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_000236.2:p.Pro773Leu
CA4448450
NM_000245.4:c.2318C>T