Canonical Allele Identifier: PA658667232
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000537898
ClinVar Variation:
460417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Leu273Pro
CA3403981
NM_003060.4:c.818T>C