Canonical Allele Identifier: PA2828022852
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Cys1360Phe
CA040240
NM_001354906.2:c.4079G>T