Canonical Allele Identifier: PA2580273789
Gene: SLC18A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1963766
ClinVar RCV Id: RCV002716147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003046.2:p.Pro140Ser
CA376718480
NM_003055.3:c.418C>T