Canonical Allele Identifier: PA286633
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys1768Glu
CA010041
NM_001127510.3:c.5302A>G