Canonical Allele Identifier: PA916020747
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000022329
ClinVar Variation:
38287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Leu210Pro
CA342637
NM_001308122.2:c.629T>C