Canonical Allele Identifier: PA2829419040
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV002022086
ClinVar Variation:
1480526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Arg227Leu
CA360804992
NM_003060.4:c.680G>T