Canonical Allele Identifier: PA916040672
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val1840Gly
CA10578404
NM_001354896.2:c.5519T>G