ClinGen Allele Registry
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Canonical Allele Identifier:
PA913201615
Gene: SLC22A5
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000022386
RCV000426334
RCV000826038
ClinVar Variation:
38794
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001295051.1:p.Arg512His
CA090920
NM_001308122.2:c.1535G>A