Canonical Allele Identifier: PA916020805
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000006792
ClinVar Variation:
6423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Trp375Arg
CA340586
NM_001308122.2:c.1123T>C
CA360806706
NM_001308122.2:c.1123T>A