Canonical Allele Identifier: PA2828042486
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp1588Asn
CA009886
NM_001354904.2:c.4762G>A