Canonical Allele Identifier: PA2827980113
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2348His
CA047019
NM_001354899.2:c.7044G>C
CA16036857
NM_001354899.2:c.7044G>T