Canonical Allele Identifier: PA2825971828
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 553477
ClinVar RCV Id: RCV000668942
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Gly292Arg
CA382898192
NM_001164278.2:c.874G>C
CA382898197
NM_001164278.2:c.874G>A