Canonical Allele Identifier: PA16039830
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg402Cys
CA10578309
NM_000038.6:c.1204C>T