Canonical Allele Identifier: PA916041794
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2803His
CA050563
NM_001354896.2:c.8407A>C