Canonical Allele Identifier: PA2825630229
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730254
ClinVar RCV Id: RCV002326430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly1109Val
CA16028628
NM_001127510.3:c.3326G>T