Canonical Allele Identifier: PA2828042057
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn1541Asp
CA040350
NM_001354904.2:c.4621A>G