Canonical Allele Identifier: PA2826554123
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_001263255.1:p.Gln348Leu
CA6077325
NM_001276326.2:c.1043A>T