Canonical Allele Identifier: PA2828023490
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gln1466His
CA16032805
NM_001354906.2:c.4398G>C
CA16032806
NM_001354906.2:c.4398G>T