Canonical Allele Identifier: PA2828076159
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 549671
ClinVar RCV Id: RCV000664211 RCV002440408
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350047.1:p.Trp99Cys
CA4938159
NM_001363118.2:c.297G>C
CA372626736
NM_001363118.2:c.297G>T