Canonical Allele Identifier: PA2825103214
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2155877
ClinVar RCV Id: RCV003090779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Thr759Ile
CA368981973
NM_000245.4:c.2276C>T