Allele Registry

Canonical Allele Identifier: PA2826374636

Gene: ANKRD11 HGNC NCBI

ClinVar Allele:

409791

ClinVar RCV:

RCV000485946

ClinVar Variation:

421226

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243111.1:p.Pro2494Thr	CA16620302 NM_001256182.2:c.7480C>A