Canonical Allele Identifier: PA2827959849
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val1786Ile
CA041569
NM_001354897.2:c.5356G>A