Canonical Allele Identifier: PA2827961783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly2380Val
CA046963
NM_001354897.2:c.7139G>T