Canonical Allele Identifier: PA2828007706
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser1035Ile
CA035157
NM_001354902.2:c.3104G>T