Canonical Allele Identifier: PA2825025069
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2816057
ClinVar RCV Id: RCV003744141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2651Asp
CA16038599
NM_000038.6:c.7952T>A