Canonical Allele Identifier: PA2827942649
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233215
ClinVar Variation Id: 862543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser1028Arg
CA10578350
NM_001354895.2:c.3084T>A
CA16028081
NM_001354895.2:c.3082A>C
CA16028087
NM_001354895.2:c.3084T>G