Canonical Allele Identifier: PA2827980627
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg2502Trp
CA013892
NM_001354899.2:c.7504C>T