Canonical Allele Identifier: PA916041663
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629969
ClinVar RCV Id: RCV000774833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly2695Cys
CA16038769
NM_001354896.2:c.8083G>T