Canonical Allele Identifier: PA2826376598
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695679
ClinVar RCV Id: RCV002265314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Val2641Met
CA397145048
NM_001256183.2:c.7921G>A