Canonical Allele Identifier: PA16040012
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Cys1727Arg
CA040871
NM_000038.6:c.5179T>C