Canonical Allele Identifier: PA2826376156
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2442504
ClinVar RCV Id: RCV003149276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243112.1:p.Ser2110Cys
CA8241494
NM_001256183.2:c.6329C>G