Canonical Allele Identifier: PA2827980859
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069385
ClinVar RCV Id: RCV004007929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2572Arg
CA16038270
NM_001354899.2:c.7715A>G