Canonical Allele Identifier: PA2825629651
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1016Val
CA16028005
NM_001127510.3:c.3047A>T