Canonical Allele Identifier: PA127771
Gene: ANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 18059
ClinVar RCV Id: RCV000019676 RCV000234999 RCV000211890 RCV000474063 RCV000620379 RCV001145853 RCV001082560 RCV000852983 RCV001841250 RCV003904850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120965.1:p.Arg1812Trp
CA127768
NM_001127493.3:c.5434C>T