Canonical Allele Identifier: PA2825642096
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1755Ile
CA16032962
NM_001127511.3:c.5264C>T