Canonical Allele Identifier: PA2825011674
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala15Val
CA16021438
NM_000038.6:c.44C>T