Canonical Allele Identifier: PA1139695506
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 846688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Pro290Leu
CA3403972
NM_001308122.2:c.869C>T