Canonical Allele Identifier: PA1139748161
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 855840
ClinVar RCV Id: RCV001061184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Ala153Thr
CA407963795
NM_033409.4:c.457G>A