Canonical Allele Identifier: PA2827999611
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2726His
CA050563
NM_001354901.2:c.8176A>C