Canonical Allele Identifier: PA2827949541
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser293Asn
CA16023237
NM_001354896.2:c.878G>A