Canonical Allele Identifier: PA2827959596
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly1712Glu
CA009865
NM_001354897.2:c.5135G>A