Canonical Allele Identifier: PA645400192
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1671Thr
CA16032296
NM_001127510.3:c.5011G>A