Canonical Allele Identifier: PA2825640109
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp1120Gly
CA035284
NM_001127511.3:c.3359A>G