Canonical Allele Identifier: PA891861881
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 574430
ClinVar RCV Id: RCV000696358
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Asp200Glu
CA382901951
NM_001164277.2:c.600C>G
CA382901952
NM_001164277.2:c.600C>A