Canonical Allele Identifier: PA2828042268
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1563Asn
CA040545
NM_001354904.2:c.4688C>A