Allele Registry

Canonical Allele Identifier: PA2826374859

Gene: ANKRD11 HGNC NCBI

ClinVar RCV:

RCV000413362

ClinVar Variation:

372597

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243112.1:p.Ala225Val	CA8243014 NM_001256183.2:c.674C>T