Canonical Allele Identifier: PA2827980462
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1449206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2452Glu
CA16037517
NM_001354899.2:c.7354C>G