Canonical Allele Identifier: PA2825972804
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6935
ClinVar RCV Id: RCV000007347 RCV000059117 RCV002482840
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Gly339Asp
CA219275
NM_001164280.2:c.1016G>A