Allele Registry

Canonical Allele Identifier: PA645436477

Gene: ANKRD11 HGNC NCBI

ClinVar RCV:

RCV000486192

ClinVar Variation:

422001

HGVS (amino-acid)	Matching Registered Transcripts
NP_037407.4:p.Arg2452Cys	CA16620303 NM_013275.6:c.7354C>T