Canonical Allele Identifier: PA1139733738
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg45Cys
CA053936
NM_001354902.2:c.133C>T