Canonical Allele Identifier: PA658829865
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 551258
ClinVar RCV Id: RCV000666266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Gly15dup
CA658821627
NM_003060.4:c.43_45dup