ClinGen Allele Registry
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Canonical Allele Identifier:
PA312957
Gene: SLC22A5
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000186146
RCV000549976
RCV000785735
RCV002307436
ClinVar Variation:
203931
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003051.1:p.Gly484Val
CA312956
NM_003060.4:c.1451G>T