Canonical Allele Identifier: PA2827768771
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315970
ClinVar RCV Id: RCV001757417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341168.1:p.Leu1077Phe
CA357935960
NM_001354239.2:c.3229C>T