Canonical Allele Identifier: PA2827942568
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1003Asn
CA007992
NM_001354895.2:c.3007G>A