Canonical Allele Identifier: PA2826941179
Gene: IBA57 HGNC NCBI

Linked Data

ClinVar Variation Id: 379988
ClinVar RCV Id: RCV000439267 RCV000676869 RCV001702642 RCV001515780 RCV001702443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001297256.1:p.Gly18Ser
CA1431197
NM_001310327.2:c.52G>A