Canonical Allele Identifier: PA658660061
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Cys1643Phe
CA040240
NM_001127510.3:c.4928G>T