Canonical Allele Identifier: PA916020824
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 529848
ClinVar RCV Id: RCV000635348 RCV001274338
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Leu433Val
CA3404101
NM_001308122.2:c.1297C>G