Canonical Allele Identifier: PA114520
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg396Cys
CA004103
NM_001127511.3:c.1186C>T