Canonical Allele Identifier: PA658808942
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 496949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Ser164Arg
CA6311826
NM_001164277.2:c.492C>A
CA382902943
NM_001164277.2:c.492C>G
CA382902974
NM_001164277.2:c.490A>C