Canonical Allele Identifier: PA2580357787
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695679
ClinVar RCV Id: RCV002265314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037407.4:p.Val2641Met
CA397145048
NM_013275.6:c.7921G>A