Canonical Allele Identifier: PA2499295110
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056779
ClinVar RCV Id: RCV001365658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Phe354Leu
CA407962530
NM_033409.4:c.1062C>G
CA407962531
NM_033409.4:c.1062C>A
CA407962536
NM_033409.4:c.1060T>C