Canonical Allele Identifier: PA2825024659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His2551Leu
CA16037955
NM_000038.6:c.7652A>T