Canonical Allele Identifier: PA2829419478
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 966759
ClinVar RCV Id: RCV001241513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Thr506Ser
CA360809832
NM_003060.4:c.1516A>T
CA360809835
NM_003060.4:c.1517C>G