Canonical Allele Identifier: PA916041356
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln2421Pro
CA10578440
NM_001354896.2:c.7262A>C