Canonical Allele Identifier: PA2828048507
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760417
ClinVar RCV Id: RCV002400793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Glu2456Asp
CA16038154
NM_001354904.2:c.7368A>C
CA16038155
NM_001354904.2:c.7368A>T