Canonical Allele Identifier: PA2741897594
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2581708
ClinVar RCV Id: RCV003330484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Pro16Leu
CA360802271
NM_003060.4:c.47C>T