Canonical Allele Identifier: PA2828036481
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn900Ser
CA16028071
NM_001354904.2:c.2699A>G