Canonical Allele Identifier: PA2827986620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 933161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg1548Ser
CA16031778
NM_001354900.2:c.4642C>A