Canonical Allele Identifier: PA2580274192
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1707665
ClinVar RCV Id: RCV002286644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Ser59Arg
CA3403805
NM_003060.4:c.177C>G
CA360802523
NM_003060.4:c.175A>C
CA360802529
NM_003060.4:c.177C>A