Canonical Allele Identifier: PA658659693
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1126Ile
CA035157
NM_001127510.3:c.3377G>T