Canonical Allele Identifier: PA342688
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV003508569
ClinVar Variation:
2725233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Val481Phe
CA342687
NM_003060.4:c.1441G>T