Canonical Allele Identifier: PA658804032
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537671
ClinVar RCV Id: RCV003653247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser40Asn
CA360612041
NM_001127511.3:c.119G>A