Canonical Allele Identifier: PA645403619
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn2785His
CA050563
NM_001127510.3:c.8353A>C