Canonical Allele Identifier: PA2825021309
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1691Thr
CA16032418
NM_000038.6:c.5071C>A