Canonical Allele Identifier: PA2826924129
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2065758
ClinVar RCV Id: RCV002958714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Arg72Gln
CA360802603
NM_001308122.2:c.215G>A