Canonical Allele Identifier: PA169269
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142731
ClinVar RCV Id: RCV000132104 RCV000590671 RCV002514750 RCV002265621 RCV003998132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg1432Gln
CA009471
NM_001127511.3:c.4295G>A