Canonical Allele Identifier: PA2828047939
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2384Ser
CA10578446
NM_001354904.2:c.7151A>G