Canonical Allele Identifier: PA645400835
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1994Val
CA043598
NM_001127510.3:c.5981A>T