Allele Registry

Canonical Allele Identifier: PA145029

Gene: ANK2 HGNC NCBI

ClinVar RCV:

RCV000589585

RCV000620213

RCV000852980

RCV001085479

RCV001150178

RCV001256867

RCV001841765

RCV003974947

ClinVar Variation:

67599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139.3:p.Val3634Asp	CA145025 NM_001148.6:c.10901T>A