Canonical Allele Identifier: PA189071
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2450Pro
CA013665
NM_001127511.3:c.7348T>C