Canonical Allele Identifier: PA2829101997
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207942
ClinVar RCV Id: RCV000190219
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Amino-acid Alleles

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