Canonical Allele Identifier: PA2827989027
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln2281Arg
CA16036522
NM_001354900.2:c.6842A>G