Canonical Allele Identifier: PA658660842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2626Asn
CA16038448
NM_001127510.3:c.7877C>A