Canonical Allele Identifier: PA2828015453
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1770136
ClinVar RCV Id: RCV002387484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.His343Tyr
CA16024219
NM_001354903.2:c.1027C>T