Canonical Allele Identifier: PA338823
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn372Asp
CA026723
NM_000038.6:c.1114A>G