Canonical Allele Identifier: PA2828375031
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2153907
ClinVar RCV Id: RCV003081517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Val343Leu
CA407962606
NM_001370085.1:c.1027G>T
CA407962607
NM_001370085.1:c.1027G>C