Canonical Allele Identifier: PA2828076331
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96702
ClinVar RCV Id: RCV000082864
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350047.1:p.Ala284Asp
CA345434
NM_001363118.2:c.851C>A