Canonical Allele Identifier: PA2825972467
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2769665
ClinVar RCV Id: RCV003507901
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Arg77Gly
CA382905862
NM_001164280.2:c.229C>G