Canonical Allele Identifier: PA2828009895
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser1751Thr
CA042221
NM_001354902.2:c.5251T>A