Canonical Allele Identifier: PA2826924090
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1909420
ClinVar RCV Id: RCV002587397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Cys50Trp
CA127196327
NM_001308122.2:c.150C>G