Canonical Allele Identifier: PA2827798805
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1739811
ClinVar RCV Id: RCV002332148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341171.1:p.Tyr1836Ser
CA357943563
NM_001354242.2:c.5507A>C