Canonical Allele Identifier: PA2827989904
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His2550Pro
CA049129
NM_001354900.2:c.7649A>C