Canonical Allele Identifier: PA1139695508
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV001242928
ClinVar Variation:
967907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Arg306Gly
CA360805538
NM_001308122.2:c.916C>G