Canonical Allele Identifier: PA2826376446
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 588960
ClinVar RCV Id: RCV002245629 RCV001868353 RCV002315453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Leu2400dup
CA624452345
NM_001256183.2:c.7198_7200dup