Canonical Allele Identifier: PA2825638065
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala422Thr
CA16024191
NM_001127511.3:c.1264G>A