Canonical Allele Identifier: PA645399058
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu922Phe
CA033363
NM_001127510.3:c.2764C>T