Canonical Allele Identifier: PA2828047820
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Leu2367Pro
CA048192
NM_001354904.2:c.7100T>C