Canonical Allele Identifier: PA2827989831
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760236
ClinVar RCV Id: RCV002400612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2528Thr
CA16038070
NM_001354900.2:c.7583G>C