Canonical Allele Identifier: PA2826373319
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 589659
ClinVar RCV Id: RCV001553267 RCV003525955 RCV002316884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243111.1:p.Ile728Met
CA8242626
NM_001256182.2:c.2184C>G