Canonical Allele Identifier: PA2828041317
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 933161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg1463Ser
CA16031778
NM_001354904.2:c.4387C>A