Canonical Allele Identifier: PA2828375020
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315574
ClinVar RCV Id: RCV001774819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Tyr329Cys
CA407962689
NM_001370085.1:c.986A>G