Canonical Allele Identifier: PA2826376507
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2957354
ClinVar RCV Id: RCV003819041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Ser2496Phe
CA397147947
NM_001256183.2:c.7487C>T