Canonical Allele Identifier: PA915985196
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6933
ClinVar RCV Id: RCV000007345 RCV000059144 RCV002482839
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Arg28His
CA219358
NM_001467.6:c.83G>A