Canonical Allele Identifier: PA2828028117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2324Asn
CA16037169
NM_001354903.2:c.6971G>A