Canonical Allele Identifier: PA2827989978
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile2574Thr
CA16038374
NM_001354900.2:c.7721T>C