Canonical Allele Identifier: PA2827953432
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2684Asn
CA16038702
NM_001354896.2:c.8051T>A