Canonical Allele Identifier: PA189072
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2468Pro
CA013665
NM_000038.6:c.7402T>C