Canonical Allele Identifier: PA2741996925
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2683525
ClinVar RCV Id: RCV003480345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Val11Ala
CA407964683
NM_033409.4:c.32T>C
CA2697547263
NM_033409.4:c.32_33delinsCT