Canonical Allele Identifier: PA2828005071
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.His1050Leu
CA035977
NM_001354905.2:c.3149A>T