Canonical Allele Identifier: PA2826374564
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2439087
ClinVar RCV Id: RCV003141422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243111.1:p.Arg2387His
CA397149129
NM_001256182.2:c.7160G>A