Canonical Allele Identifier: PA2825022482
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1992Ser
CA043556
NM_000038.6:c.5974C>T