Canonical Allele Identifier: PA2828012496
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2362Arg
CA16037774
NM_001354905.2:c.7085C>G