Canonical Allele Identifier: PA2827992039
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 942507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val391Met
CA16024254
NM_001354901.2:c.1171G>A