Canonical Allele Identifier: PA336549
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg1146Cys
CA035367
NM_000038.6:c.3436C>T