Canonical Allele Identifier: PA2827981790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg35Ser
CA16021946
NM_001354900.2:c.103C>A