Canonical Allele Identifier: PA2573225484
Gene: SLC18A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380855
ClinVar RCV Id: RCV001895081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003046.2:p.Val37Ala
CA376715827
NM_003055.3:c.110T>C