Canonical Allele Identifier: PA2829335041
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551319
ClinVar RCV Id: RCV000666350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Trp128Arg
CA382904273
NM_001467.6:c.382T>C
CA382904277
NM_001467.6:c.382T>A