Canonical Allele Identifier: PA145029
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139.3:p.Val3634Asp
CA145025
NM_001148.6:c.10901T>A