Canonical Allele Identifier: PA2827254678
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1798731
ClinVar RCV Id: RCV002435702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Val554Leu
CA368987173
NM_001324402.2:c.1660G>T
CA368987178
NM_001324402.2:c.1660G>C