Canonical Allele Identifier: PA2827977722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Cys1615Phe
CA040240
NM_001354899.2:c.4844G>T