Canonical Allele Identifier: PA2825972792
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551256
ClinVar RCV Id: RCV000666264
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Trp330Ser
CA6311643
NM_001164280.2:c.989G>C