Canonical Allele Identifier: PA658832745
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 558209
ClinVar RCV Id: RCV000674442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Glu190Asp
CA382902093
NM_001164277.2:c.570A>T
CA382902094
NM_001164277.2:c.570A>C