Canonical Allele Identifier: PA2828018850
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser727Asn
CA348296
NM_001354906.2:c.2180G>A