Canonical Allele Identifier: PA2827975648
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727379
ClinVar RCV Id: RCV002319894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1000Gly
CA16028082
NM_001354899.2:c.2998A>G