Canonical Allele Identifier: PA2825024616
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2540Ala
CA16037879
NM_000038.6:c.7618C>G