Allele Registry

Canonical Allele Identifier: PA645436478

Gene: ANKRD11 HGNC NCBI

ClinVar Allele:

409791

ClinVar RCV:

RCV000485946

ClinVar Variation:

421226

HGVS (amino-acid)	Matching Registered Transcripts
NP_037407.4:p.Pro2494Thr	CA16620302 NM_013275.6:c.7480C>A