Canonical Allele Identifier: PA2828028962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.His2450Leu
CA16037955
NM_001354903.2:c.7349A>T