Canonical Allele Identifier: PA2825972299
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 554828
ClinVar RCV Id: RCV000670525
ClinVar Variation Id: 1366825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Ser319Arg
CA6311601
NM_001164279.2:c.957T>G
CA382894369
NM_001164279.2:c.957T>A
CA382894379
NM_001164279.2:c.955A>C