Canonical Allele Identifier: PA916041551
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 801041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2598Ala
CA16038136
NM_001354896.2:c.7792T>G