Canonical Allele Identifier: PA916041990
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp993Asn
CA008010
NM_001354898.2:c.2977G>A