Canonical Allele Identifier: PA916041359
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2423His
CA16037039
NM_001354896.2:c.7267A>C