Canonical Allele Identifier: PA2828028552
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp2389Asn
CA013697
NM_001354903.2:c.7165G>A