Canonical Allele Identifier: PA2826924023
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2825804
ClinVar RCV Id: RCV003616440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Gly15Arg
CA360802262
NM_001308122.2:c.43G>A
CA360802263
NM_001308122.2:c.43G>C