Canonical Allele Identifier: PA2825641832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2726739
ClinVar RCV Id: RCV003539003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1674Ile
CA16032429
NM_001127511.3:c.5021C>T