Canonical Allele Identifier: PA2828028610
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2396Trp
CA16037624
NM_001354903.2:c.7187C>G