Canonical Allele Identifier: PA2825022143
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 422390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1908Ser
CA16033859
NM_000038.6:c.5723A>G