Canonical Allele Identifier: PA2827981068
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2635Gly
CA16038681
NM_001354899.2:c.7904A>G