Canonical Allele Identifier: PA916041308
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2387Ser
CA046951
NM_001354896.2:c.7159C>T