Canonical Allele Identifier: PA2828027743
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1377591
ClinVar RCV Id: RCV003772642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Tyr2265His
CA16036787
NM_001354903.2:c.6793T>C