Canonical Allele Identifier: PA915985326
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68283
ClinVar RCV Id: RCV000059134
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Cys176Arg
CA219328
NM_001467.6:c.526T>C