Canonical Allele Identifier: PA891848622
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 580421
ClinVar RCV Id: RCV000703959 RCV002226488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Trp14Arg
CA127196122
NM_003060.4:c.40T>A
CA360802255
NM_003060.4:c.40T>C