Canonical Allele Identifier: PA2825972713
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2181223
ClinVar RCV Id: RCV002606034
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Met266Val
CA382900558
NM_001164280.2:c.796A>G