Canonical Allele Identifier: PA2826376480
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 429712
ClinVar RCV Id: RCV000493430 RCV002275041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Arg2452Gly
CA397148533
NM_001256183.2:c.7354C>G