Canonical Allele Identifier: PA645400205
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1691Thr
CA16032418
NM_001127510.3:c.5071C>A