Canonical Allele Identifier: PA2825971734
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6936
ClinVar RCV Id: RCV000007348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Gly209Ser
CA382901791
NM_001164278.2:c.625G>A