Canonical Allele Identifier: PA2826374708
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 429654
ClinVar RCV Id: RCV000493206 RCV001251206 RCV003403140 RCV003766774
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243111.1:p.Leu2605Arg
CA397145398
NM_001256182.2:c.7814T>G