Canonical Allele Identifier: PA2827964569
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg389Ser
CA10578311
NM_001354898.2:c.1165C>A