Canonical Allele Identifier: PA2826374707
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1303861
ClinVar RCV Id: RCV001758154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243111.1:p.Leu2606del
CA2580613925
NM_001256182.2:c.7816_7818del