Canonical Allele Identifier: PA2827989945
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 654022
ClinVar RCV Id: RCV003653372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu2562Asp
CA16038295
NM_001354900.2:c.7686A>C
CA16038296
NM_001354900.2:c.7686A>T