Canonical Allele Identifier: PA916041653
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 565362
ClinVar RCV Id: RCV004026176 RCV003534550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2683Ser
CA16038695
NM_001354896.2:c.8047C>T