Canonical Allele Identifier: PA2828044219
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1477212
ClinVar RCV Id: RCV003773118
ClinVar Variation Id: 2452715
ClinVar RCV Id: RCV003177489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp1822Glu
CA16034112
NM_001354904.2:c.5466T>A
CA16034113
NM_001354904.2:c.5466T>G