Canonical Allele Identifier: PA891855138
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 581134
ClinVar RCV Id: RCV000704874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Met317Thr
CA407962763
NM_033409.4:c.950T>C