Canonical Allele Identifier: PA2828030338
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2502His
CA050563
NM_001354906.2:c.7504A>C