Canonical Allele Identifier: PA2827975623
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042543
ClinVar RCV Id: RCV002242366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp990Tyr
CA16028017
NM_001354899.2:c.2968G>T