Canonical Allele Identifier: PA2827962618
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551
ClinVar RCV Id: RCV000775753 RCV003493584 RCV003766599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr2633Ala
CA16038426
NM_001354897.2:c.7897A>G