Canonical Allele Identifier: PA2825103249
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 849997
ClinVar RCV Id: RCV001054072 RCV002451224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Asn778Thr
CA368982413
NM_000245.4:c.2333A>C