Canonical Allele Identifier: PA2825972582
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 215178
ClinVar RCV Id: RCV000199219 RCV001084902 RCV001027800 RCV003224223 RCV003955196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Arg166His
CA323754
NM_001164280.2:c.497G>A