Canonical Allele Identifier: PA2829100787
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 191416
ClinVar RCV Id: RCV001842514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373095.1:p.Val2695Leu
CA199816
NM_001386166.1:c.8083G>C
CA357943476
NM_001386166.1:c.8083G>T