Canonical Allele Identifier: PA2827983802
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn700Ser
CA007300
NM_001354900.2:c.2099A>G