Canonical Allele Identifier: PA2828010165
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1856Ala
CA010734
NM_001354902.2:c.5566A>G