Canonical Allele Identifier: PA2828374802
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 145
ClinVar RCV Id: RCV000000168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Pro28Thr
CA339798
NM_001370085.1:c.82C>A