Canonical Allele Identifier: PA916041671
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132756
ClinVar RCV Id: RCV000575859 RCV000588854 RCV003997305 RCV003764829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2698Ala
CA014255
NM_001354896.2:c.8092C>G