Canonical Allele Identifier: PA2828029421
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2525Asn
CA16038448
NM_001354903.2:c.7574C>A