Canonical Allele Identifier: PA2827945539
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.His1897Pro
CA010592
NM_001354895.2:c.5690A>C