Canonical Allele Identifier: PA2827951091
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181770
ClinVar RCV Id: RCV000159511 RCV001020050 RCV003534396 RCV003998393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1134Asp
CA008298
NM_001354896.2:c.3401G>A