Canonical Allele Identifier: PA916042228
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly277Glu
CA049608
NM_001354902.2:c.830G>A