Canonical Allele Identifier: PA2573217954
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350835
ClinVar RCV Id: RCV002042166
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Arg319Pro
CA382897341
NM_001467.6:c.956G>C