Canonical Allele Identifier: PA2827962392
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2065558
ClinVar RCV Id: RCV003744826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His2564Arg
CA16037976
NM_001354897.2:c.7691A>G