Canonical Allele Identifier: PA2825645216
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn2767His
CA050563
NM_001127511.3:c.8299A>C