Canonical Allele Identifier: PA916041989
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp999Gly
CA034127
NM_001354897.2:c.2996A>G