Canonical Allele Identifier: PA2828041192
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp1444Glu
CA10578381
NM_001354904.2:c.4332T>A
CA16031660
NM_001354904.2:c.4332T>G