Canonical Allele Identifier: PA2573225488
Gene: SLC18A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390102
ClinVar RCV Id: RCV001890834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003046.2:p.Asp46Gly
CA376716009
NM_003055.3:c.137A>G