Canonical Allele Identifier: PA2826373673
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 798243
ClinVar RCV Id: RCV001333688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243111.1:p.Thr1318Ser
CA8242245
NM_001256182.2:c.3953C>G
CA397158639
NM_001256182.2:c.3952A>T