Canonical Allele Identifier: PA2825018138
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1016Val
CA16028005
NM_000038.6:c.3047A>T