Canonical Allele Identifier: PA645436480
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_037407.4:p.Leu2605Arg
CA397145398
NM_013275.6:c.7814T>G