Canonical Allele Identifier: PA658832759
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 558464
ClinVar RCV Id: RCV000674738
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Cys242Ser
CA382901184
NM_001164277.2:c.725G>C
CA382901198
NM_001164277.2:c.724T>A