Canonical Allele Identifier: PA916041463
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu2511Pro
CA048192
NM_001354896.2:c.7532T>C