Canonical Allele Identifier: PA2826375163
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2911788
ClinVar RCV Id: RCV003642228 RCV004527007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Arg730Lys
CA397162983
NM_001256183.2:c.2189G>A