Canonical Allele Identifier: PA915988110
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 554828
ClinVar RCV Id: RCV000670525
ClinVar Variation Id: 1366825
ClinVar RCV Id: RCV001962157 RCV002506916 RCV002550382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ser414Arg
CA6311601
NM_001164278.2:c.1242T>G
CA382894369
NM_001164278.2:c.1242T>A
CA382894379
NM_001164278.2:c.1240A>C