Canonical Allele Identifier: PA2827966414
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp978Asn
CA007992
NM_001354898.2:c.2932G>A