Canonical Allele Identifier: PA145028
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_001120965.1:p.Val1540Asp
CA145025
NM_001127493.3:c.4619T>A