Canonical Allele Identifier: PA2827949748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn372Asp
CA026723
NM_001354896.2:c.1114A>G