Canonical Allele Identifier: PA2828023996
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1551Ile
CA042161
NM_001354906.2:c.4651G>A