Canonical Allele Identifier: PA2827972295
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2760His
CA050563
NM_001354898.2:c.8278A>C