Canonical Allele Identifier: PA916040611
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1796Arg
CA16032991
NM_001354896.2:c.5387C>G