Canonical Allele Identifier: PA2828029029
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760417
ClinVar RCV Id: RCV002400793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Glu2299Asp
CA16038154
NM_001354906.2:c.6897A>C
CA16038155
NM_001354906.2:c.6897A>T