Canonical Allele Identifier: PA2827971730
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile2590Val
CA336774
NM_001354898.2:c.7768A>G