Canonical Allele Identifier: PA2827973597
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn344Asp
CA026723
NM_001354899.2:c.1030A>G