Canonical Allele Identifier: PA915976537
Gene: SLC18A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 732977
ClinVar RCV Id: RCV000908188 RCV001334112 RCV003895522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003046.2:p.Arg29Trp
CA5496683
NM_003055.3:c.85C>T