Canonical Allele Identifier: PA2827989908
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His2550Asp
CA16038213
NM_001354900.2:c.7648C>G