Canonical Allele Identifier: PA093861
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13882
ClinVar RCV Id: RCV000014896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Val1188Leu
CA256994
NM_000245.4:c.3562G>T
CA368990990
NM_000245.4:c.3562G>C