Canonical Allele Identifier: PA2826373310
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3030131
ClinVar RCV Id: RCV003899376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243111.1:p.Glu707Lys
CA397163150
NM_001256182.2:c.2119G>A