Canonical Allele Identifier: PA2827982920
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro382Thr
CA16024197
NM_001354900.2:c.1144C>A