Canonical Allele Identifier: PA2827945371
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser1842Thr
CA042221
NM_001354895.2:c.5524T>A