Canonical Allele Identifier: PA2827982696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn313Asp
CA026723
NM_001354900.2:c.937A>G