Canonical Allele Identifier: PA2827966467
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1001Ser
CA16028071
NM_001354898.2:c.3002A>G