Canonical Allele Identifier: PA2827940847
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411398
ClinVar Variation Id: 485101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.His444Gln
CA027188
NM_001354895.2:c.1332T>G
CA16024222
NM_001354895.2:c.1332T>A