Canonical Allele Identifier: PA2826376447
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1254565
ClinVar RCV Id: RCV001658747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Leu2400Val
CA286509453
NM_001256183.2:c.7198C>G