Canonical Allele Identifier: PA658660085
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1689Ile
CA040566
NM_001127510.3:c.5066C>T