Canonical Allele Identifier: PA658682326
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 476611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Asp174Gly
CA9724760
NM_033409.4:c.521A>G