Canonical Allele Identifier: PA199820
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_001139.3:p.Val3895Leu
CA199816
NM_001148.6:c.11683G>C
CA357943476
NM_001148.6:c.11683G>T