Canonical Allele Identifier: PA2829101997
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207942
ClinVar RCV Id: RCV000190219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373103.1:p.Lys1673Glu
CA204253
NM_001386174.1:c.5017A>G