Canonical Allele Identifier: PA645400550
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1842Thr
CA042221
NM_001127510.3:c.5524T>A