Canonical Allele Identifier: PA645399553
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1142Thr
CA035313
NM_001127510.3:c.3425A>C