Canonical Allele Identifier: PA2826376583
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718852
ClinVar RCV Id: RCV002301743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Arg2608Gly
CA397145365
NM_001256183.2:c.7822C>G