Canonical Allele Identifier: PA916040512
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1716Asn
CA040634
NM_001354896.2:c.5146G>A