Canonical Allele Identifier: PA2825642087
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1035716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys1752Asn
CA16032941
NM_001127511.3:c.5256G>C
CA16032942
NM_001127511.3:c.5256G>T