Canonical Allele Identifier: PA2827987453
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro1802Thr
CA16033423
NM_001354900.2:c.5404C>A