Canonical Allele Identifier: PA658655191
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 445552
ClinVar RCV Id: RCV000513899 RCV002316459 RCV002466525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243111.1:p.Ser739Leu
CA8242615
NM_001256182.2:c.2216C>T