Canonical Allele Identifier: PA2826924103
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1491545
ClinVar RCV Id: RCV002010096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Asn57Lys
CA360802516
NM_001308122.2:c.171C>A
CA360802517
NM_001308122.2:c.171C>G