Canonical Allele Identifier: PA2827956650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val831Ile
CA007489
NM_001354897.2:c.2491G>A