Canonical Allele Identifier: PA2825640117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro1122Arg
CA16028829
NM_001127511.3:c.3365C>G