Canonical Allele Identifier: PA2827964439
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn347Asp
CA026723
NM_001354898.2:c.1039A>G