Canonical Allele Identifier: PA204261
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207944
ClinVar RCV Id: RCV000190221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139.3:p.Val2708Ala
CA204259
NM_001148.6:c.8123T>C