Allele Registry

Canonical Allele Identifier: PA2826374612

Gene: ANKRD11 HGNC NCBI

ClinVar RCV:

RCV000486192

ClinVar Variation:

422001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243111.1:p.Arg2452Cys	CA16620303 NM_001256182.2:c.7354C>T