Canonical Allele Identifier: PA2827995862
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Cys1584Phe
CA040240
NM_001354901.2:c.4751G>T