Canonical Allele Identifier: PA2825387294
Gene: SLC22A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3163328
ClinVar RCV Id: RCV004448711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034841.3:p.Arg256Gln
CA6061227
NM_001039752.4:c.767G>A