Canonical Allele Identifier: PA2827980935
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949059
ClinVar RCV Id: RCV003650741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2597Asn
CA16038441
NM_001354899.2:c.7790G>A