Canonical Allele Identifier: PA2828029364
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn2517Asp
CA338662
NM_001354903.2:c.7549A>G