Canonical Allele Identifier: PA2828023370
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2726739
ClinVar RCV Id: RCV003539003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1591Ile
CA16032429
NM_001354903.2:c.4772C>T