Canonical Allele Identifier: PA2828048638
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069385
ClinVar RCV Id: RCV004007929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gln2474Arg
CA16038270
NM_001354904.2:c.7421A>G