Canonical Allele Identifier: PA2827981045
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 495374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2628Gly
CA16038634
NM_001354899.2:c.7883A>G