Canonical Allele Identifier: PA2828009897
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1752Thr
CA16033423
NM_001354902.2:c.5254C>A