Canonical Allele Identifier: PA916041670
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411462
ClinVar RCV Id: RCV000585717 RCV004001953 RCV003651868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2698Ser
CA16038785
NM_001354896.2:c.8092C>T