Canonical Allele Identifier: PA2825017013
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg845Cys
CA16026883
NM_000038.6:c.2533C>T