Canonical Allele Identifier: PA284852
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6921
ClinVar RCV Id: RCV000007330 RCV000059116
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Gly339Cys
CA284849
NM_001467.6:c.1015G>T