Canonical Allele Identifier: PA645502897
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000225039
ClinVar Variation:
236195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Glu220Val
CA10581560
NM_003060.4:c.659A>T