Canonical Allele Identifier: PA108097
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 6422
ClinVar RCV Id: RCV000006791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Arg169Trp
CA340585
NM_003060.4:c.505C>T