Canonical Allele Identifier: PA2827971042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2380His
CA16037039
NM_001354898.2:c.7138A>C