Canonical Allele Identifier: PA2828044974
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser1918Asn
CA043925
NM_001354904.2:c.5753G>A