Canonical Allele Identifier: PA2828037988
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.His1084Leu
CA035977
NM_001354904.2:c.3251A>T