Canonical Allele Identifier: PA2828049855
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2659His
CA050563
NM_001354904.2:c.7975A>C