Canonical Allele Identifier: PA2573225649
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439444
ClinVar RCV Id: RCV001965299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Trp14Cys
CA360802260
NM_003060.4:c.42G>T
CA360802261
NM_003060.4:c.42G>C