Canonical Allele Identifier: PA2828004232
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 492672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala2485Thr
CA16038108
NM_001354902.2:c.7453G>A