Canonical Allele Identifier: PA145029
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67599
ClinVar RCV Id: RCV000589585 RCV000620213 RCV000852980 RCV001150178 RCV001085479 RCV001841765 RCV001256867 RCV003974947
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Amino-acid Alleles

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