Canonical Allele Identifier: PA2825014077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser293Asn
CA16023237
NM_000038.6:c.878G>A