Canonical Allele Identifier: PA2825018139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1315725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1016Tyr
CA16028002
NM_000038.6:c.3046G>T