Canonical Allele Identifier: PA2741897548
Gene: SLC18A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2985423
ClinVar RCV Id: RCV003848550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003046.2:p.Asp152Glu
CA376718671
NM_003055.3:c.456C>A
CA376718674
NM_003055.3:c.456C>G