Canonical Allele Identifier: PA099669
Gene: SLC22A12 HGNC NCBI

Linked Data

ClinVar Variation Id: 3516
ClinVar RCV Id: RCV000003693 RCV000826151 RCV002512717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653186.2:p.Arg90His
CA116317
NM_144585.4:c.269G>A