Canonical Allele Identifier: PA916040454
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Cys1661Phe
CA040240
NM_001354896.2:c.4982G>T