Canonical Allele Identifier: PA1139677594
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 960489
ClinVar RCV Id: RCV001234021 RCV003166440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Phe804Ser
CA368982564
NM_001127500.3:c.2411T>C