Canonical Allele Identifier: PA2828028431
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp2207Asn
CA013697
NM_001354906.2:c.6619G>A