Canonical Allele Identifier: PA2826376504
Gene: ANKRD11 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Pro2494Thr
CA16620302
NM_001256183.2:c.7480C>A