Canonical Allele Identifier: PA2827979948
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2294Arg
CA16036522
NM_001354899.2:c.6881A>G