Allele Registry

Canonical Allele Identifier: PA300695

Gene: ANK2 HGNC NCBI

ClinVar RCV:

RCV000631636

RCV001721096

RCV002426806

ClinVar Variation:

190522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120965.1:p.Thr694Ile	CA300692 NM_001127493.3:c.2081C>T