Canonical Allele Identifier: PA2825629653
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1315725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1016Tyr
CA16028002
NM_001127510.3:c.3046G>T