Canonical Allele Identifier: PA16040056
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1994Val
CA043598
NM_000038.6:c.5981A>T