Canonical Allele Identifier: PA2573197643
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488980
ClinVar RCV Id: RCV001980402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Tyr516Cys
CA360809678
NM_001308122.2:c.1547A>G