Canonical Allele Identifier: PA915966567
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411918
ClinVar RCV Id: RCV000476062 RCV001018130 RCV001312218 RCV001788226 RCV001755706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Pro991Ser
CA4448619
NM_000245.4:c.2971C>T