Canonical Allele Identifier: PA916040866
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2004Leu
CA043504
NM_001354896.2:c.6011C>T