Canonical Allele Identifier: PA2827996513
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser1783Thr
CA042221
NM_001354901.2:c.5347T>A