Canonical Allele Identifier: PA916020795
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 460421
ClinVar RCV Id: RCV000529397 RCV001274336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Pro339Leu
CA3404012
NM_001308122.2:c.1016C>T