Canonical Allele Identifier: PA2829335060
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2910297
ClinVar RCV Id: RCV003619009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Trp138Arg
CA382903845
NM_001467.6:c.412T>C
CA382903848
NM_001467.6:c.412T>A