Canonical Allele Identifier: PA2826375964
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2804553
ClinVar RCV Id: RCV003641384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Glu1932Val
CA397152804
NM_001256183.2:c.5795A>T