Canonical Allele Identifier: PA916040916
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2054Asn
CA16034696
NM_001354896.2:c.6160G>A