Canonical Allele Identifier: PA2827966787
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1093His
CA16028675
NM_001354898.2:c.3277A>C