Canonical Allele Identifier: PA2826375153
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2574043
ClinVar RCV Id: RCV003459830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Glu709Asp
CA397163128
NM_001256183.2:c.2127A>C
CA397163129
NM_001256183.2:c.2127A>T