Canonical Allele Identifier: PA645400203
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1689Asn
CA040545
NM_001127510.3:c.5066C>A