Canonical Allele Identifier: PA346986
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210021
ClinVar RCV Id: RCV000191966
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Ala312Val
CA346985
NM_033409.4:c.935C>T