Canonical Allele Identifier: PA2828022171
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587035
ClinVar RCV Id: RCV003339112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn1252His
CA16031412
NM_001354906.2:c.3754A>C