Canonical Allele Identifier: PA2827971930
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1391692
ClinVar RCV Id: RCV003653511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2648Lys
CA16038745
NM_001354898.2:c.7943G>A