Canonical Allele Identifier: PA099678
Gene: SLC22A12 HGNC NCBI

Linked Data

ClinVar Variation Id: 305239
ClinVar RCV Id: RCV000348762 RCV003546509 RCV003409469 RCV003993926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653186.2:p.Gln382Leu
CA6077325
NM_144585.4:c.1145A>T