Canonical Allele Identifier: PA2573225643
Gene: SLC22A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424263
ClinVar RCV Id: RCV001921518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003050.2:p.Leu515Phe
CA3403716
NM_003059.3:c.1543C>T