Canonical Allele Identifier: PA2827950774
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1315725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1034Tyr
CA16028002
NM_001354896.2:c.3100G>T