Canonical Allele Identifier: PA915988072
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 199062
ClinVar RCV Id: RCV000180561 RCV000559346 RCV002408783 RCV003937641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ser378Thr
CA203733
NM_001164278.2:c.1133G>C