Canonical Allele Identifier: PA2826376579
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 429654
ClinVar RCV Id: RCV000493206 RCV001251206 RCV003403140 RCV003766774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Leu2605Arg
CA397145398
NM_001256183.2:c.7814T>G