Canonical Allele Identifier: PA2825024852
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069385
ClinVar RCV Id: RCV004007929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln2600Arg
CA16038270
NM_000038.6:c.7799A>G