Canonical Allele Identifier: PA2827977972
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly1693Asp
CA10578397
NM_001354899.2:c.5078G>A