Canonical Allele Identifier: PA256996
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_001120972.1:p.Val1206Leu
CA256994
NM_001127500.3:c.3616G>T
CA368990990
NM_001127500.3:c.3616G>C