Canonical Allele Identifier: PA2580490060
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1992208
ClinVar RCV Id: RCV002814319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Gly146Arg
CA407963837
NM_033409.4:c.436G>C
CA407963838
NM_033409.4:c.436G>A