Canonical Allele Identifier: PA658829879
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 555629
ClinVar RCV Id: RCV000671487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Gly267Glu
CA3403975
NM_003060.4:c.800G>A