Canonical Allele Identifier: PA2825018906
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 581688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1133Asn
CA16028776
NM_000038.6:c.3397G>A