Canonical Allele Identifier: PA215494
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile526Thr
CA005403
NM_001127511.3:c.1577T>C