Canonical Allele Identifier: PA2580273867
Gene: SLC18A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2177140
ClinVar RCV Id: RCV002610377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003046.2:p.Phe307Leu
CA376721189
NM_003055.3:c.919T>C
CA376721206
NM_003055.3:c.921C>A
CA376721208
NM_003055.3:c.921C>G