Canonical Allele Identifier: PA916020771
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000022344
ClinVar Variation:
25391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Arg281Trp
CA312947
NM_001308122.2:c.841C>T