Canonical Allele Identifier: PA2827986798
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Cys1602Phe
CA040240
NM_001354900.2:c.4805G>T