Canonical Allele Identifier: PA916042508
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro980Arg
CA16028829
NM_001354905.2:c.2939C>G