Canonical Allele Identifier: PA2828007389
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1529Asn
CA040545
NM_001354905.2:c.4586C>A