Canonical Allele Identifier: PA095759
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Glu36Lys
CA339796
NM_033409.4:c.106G>A