Canonical Allele Identifier: PA2825642498
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 422390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1890Ser
CA16033859
NM_001127511.3:c.5669A>G