Canonical Allele Identifier: PA297733
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg396His
CA004108
NM_001127511.3:c.1187G>A