Canonical Allele Identifier: PA916041997
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Tyr999Asp
CA16028076
NM_001354899.2:c.2995T>G