Canonical Allele Identifier: PA2573295990
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477733
ClinVar RCV Id: RCV001998435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Ala276Val
CA407963019
NM_033409.4:c.827C>T