Canonical Allele Identifier: PA2825643933
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2351Ser
CA046951
NM_001127511.3:c.7051C>T