Canonical Allele Identifier: PA1139695991
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 836693
ClinVar RCV Id: RCV001037880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Leu531Phe
CA3404186
NM_001308122.2:c.1593G>C
CA360809844
NM_001308122.2:c.1593G>T