Canonical Allele Identifier: PA2826362028
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245818
ClinVar RCV Id: RCV000237012
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240745.1:p.Val36Gly
CA10584287
NM_001253816.2:c.107T>G