Canonical Allele Identifier: PA2827974698
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn713Ser
CA007300
NM_001354899.2:c.2138A>G