Canonical Allele Identifier: PA2825644627
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2792747
ClinVar RCV Id: RCV003745809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn2575His
CA16038225
NM_001127511.3:c.7723A>C