Canonical Allele Identifier: PA916020858
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 657702
ClinVar RCV Id: RCV000814366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Pro542Ala
CA3404195
NM_001308122.2:c.1624C>G