Canonical Allele Identifier: PA2826374253
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2883204
ClinVar RCV Id: RCV003640808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243111.1:p.Ser2067Gly
CA397151764
NM_001256182.2:c.6199A>G