Canonical Allele Identifier: PA2825019981
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln1367Arg
CA16030311
NM_000038.6:c.4100A>G