Canonical Allele Identifier: PA2828016001
Gene: APC HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser269Pro
CA16024924
NM_001354906.2:c.805T>C