Canonical Allele Identifier: PA2827980216
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2377His
CA16037039
NM_001354899.2:c.7129A>C