Canonical Allele Identifier: PA2826375172
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 445552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Ser739Leu
CA8242615
NM_001256183.2:c.2216C>T