Canonical Allele Identifier: PA2825017874
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2058749
ClinVar RCV Id: RCV003744821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly974Asp
CA16027713
NM_000038.6:c.2921G>A