Canonical Allele Identifier: PA2828037392
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro1014Arg
CA16028829
NM_001354904.2:c.3041C>G