Canonical Allele Identifier: PA2825643920
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1377591
ClinVar RCV Id: RCV003772642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Tyr2348His
CA16036787
NM_001127511.3:c.7042T>C