Canonical Allele Identifier: PA658682327
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 476612
ClinVar Variation Id: 852705
ClinVar RCV Id: RCV001057369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Ser175Arg
CA9724759
NM_033409.4:c.525C>A
CA407963661
NM_033409.4:c.525C>G
CA407963667
NM_033409.4:c.523A>C