Canonical Allele Identifier: PA2828016663
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp550Gly
CA16025584
NM_001354903.2:c.1649A>G