Canonical Allele Identifier: PA2827981468
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2757His
CA050563
NM_001354899.2:c.8269A>C