Canonical Allele Identifier: PA2825644489
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His2533Leu
CA16037955
NM_001127511.3:c.7598A>T