Canonical Allele Identifier: PA2826376429
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504496
ClinVar RCV Id: RCV003231957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.His2383_Pro2384delinsGlnThr
CA2580613926
NM_001256183.2:c.7149_7150delinsAA