Canonical Allele Identifier: PA2825972069
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 552896
ClinVar RCV Id: RCV000668245
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Glu141del
CA658823058
NM_001164279.2:c.421_423del