Canonical Allele Identifier: PA2825640091
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 581688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp1115Asn
CA16028776
NM_001127511.3:c.3343G>A