Canonical Allele Identifier: PA2573090172
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1303861
ClinVar RCV Id: RCV001758154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037407.4:p.Leu2606del
CA2580613925
NM_013275.6:c.7816_7818del