Canonical Allele Identifier: PA2828029640
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly2389Val
CA16038743
NM_001354906.2:c.7166G>T