Canonical Allele Identifier: PA2741897576
Gene: SLC22A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2722859
ClinVar RCV Id: RCV003559114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003050.2:p.Asn210Lys
CA3403457
NM_003059.3:c.630C>G
CA360804101
NM_003059.3:c.630C>A