Canonical Allele Identifier: PA2829107643
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 222497
ClinVar RCV Id: RCV000208430 RCV000412995 RCV000619380 RCV000764530 RCV001252393 RCV001078702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373116.1:p.His1497Gln
CA074011
NM_001386187.2:c.4491T>G
CA357941445
NM_001386187.2:c.4491T>A