Canonical Allele Identifier: PA2828006540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1371His
CA16031385
NM_001354905.2:c.4111A>C