Canonical Allele Identifier: PA2828035873
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.His787Arg
CA033216
NM_001354904.2:c.2360A>G