Canonical Allele Identifier: PA2829100801
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1739811
ClinVar RCV Id: RCV002332148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373095.1:p.Tyr2707Ser
CA357943563
NM_001386166.1:c.8120A>C