Canonical Allele Identifier: PA2825971309
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 662077
ClinVar RCV Id: RCV000819639 RCV001729714
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Arg286Gln
CA6311715
NM_001164277.2:c.857G>A