Canonical Allele Identifier: PA2827963051
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185492
ClinVar Variation Id: 428124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Glu2760Lys
CA014471
NM_001354897.2:c.8277_8278delinsTA
CA16039228
NM_001354897.2:c.8278G>A