Canonical Allele Identifier: PA916041827
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2828Ser
CA015484
NM_001354896.2:c.8483A>G