Canonical Allele Identifier: PA127772
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 18059
ClinVar RCV Id: RCV000019676 RCV000234999 RCV000211890 RCV000474063 RCV000620379 RCV001145853 RCV001082560 RCV000852983 RCV001841250 RCV003904850
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066187.2:p.Arg1821Trp
CA127768
NM_020977.5:c.5461C>T