Canonical Allele Identifier: PA2826376582
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 803285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Arg2608Trp
CA397145367
NM_001256183.2:c.7822C>T