Canonical Allele Identifier: PA2828004101
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu2402Pro
CA048192
NM_001354902.2:c.7205T>C