Canonical Allele Identifier: PA2828029248
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2335Asp
CA338662
NM_001354906.2:c.7003A>G