Canonical Allele Identifier: PA2825971302
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2585455
ClinVar RCV Id: RCV003338071
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Val271Asp
CA382900419
NM_001164277.2:c.812T>A