Canonical Allele Identifier: PA2827945578
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 422390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn1908Ser
CA16033859
NM_001354895.2:c.5723A>G