Canonical Allele Identifier: PA156821
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1003Asn
CA007992
NM_000038.6:c.3007G>A