Canonical Allele Identifier: PA2829101013
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67596
ClinVar RCV Id: RCV000058341 RCV000794010 RCV000779424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373096.1:p.Trp335Arg
CA300933
NM_001386167.1:c.1003T>A
CA357941392
NM_001386167.1:c.1003T>C