Canonical Allele Identifier: PA915988213
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_001157751.1:p.Arg93His
CA323754
NM_001164279.2:c.278G>A