Canonical Allele Identifier: PA2825639749
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1008Ser
CA16028071
NM_001127511.3:c.3023A>G