Canonical Allele Identifier: PA2741897587
Gene: SLC22A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2780735
ClinVar RCV Id: RCV003659576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003050.2:p.Leu505Ile
CA360813176
NM_003059.3:c.1513C>A