Canonical Allele Identifier: PA916020775
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 555629
ClinVar RCV Id: RCV000671487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Gly291Glu
CA3403975
NM_001308122.2:c.872G>A