Canonical Allele Identifier: PA2827995838
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 183069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp1577Tyr
CA009798
NM_001354901.2:c.4729G>T