Canonical Allele Identifier: PA2827945115
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn1761Ser
CA041233
NM_001354895.2:c.5282A>G