Canonical Allele Identifier: PA2825103261
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 3011851
ClinVar RCV Id: RCV003872914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Asn785Ile
CA368982545
NM_000245.4:c.2354A>T