Canonical Allele Identifier: PA2827990443
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185492
ClinVar Variation Id: 428124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu2709Lys
CA014471
NM_001354900.2:c.8124_8125delinsTA
CA16039228
NM_001354900.2:c.8125G>A