Canonical Allele Identifier: PA108271
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000022340
ClinVar Variation:
25387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Gly242Val
CA342645
NM_003060.4:c.725G>T