Canonical Allele Identifier: PA127766
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 18056
ClinVar RCV Id: RCV000170702 RCV000171737 RCV000244762 RCV000845369 RCV001002092 RCV000019672 RCV000019673 RCV000058356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120965.1:p.Glu1449Gly
CA127763
NM_001127493.3:c.4346A>G