Canonical Allele Identifier: PA2827977920
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 924017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1678Pro
CA16032513
NM_001354899.2:c.5032T>C