Canonical Allele Identifier: PA2580274113
Gene: SLC22A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2080855
ClinVar RCV Id: RCV003002246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003050.2:p.Met487Thr
CA3403699
NM_003059.3:c.1460T>C