Canonical Allele Identifier: PA916040448
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133531
ClinVar RCV Id: RCV000120041 RCV000164191 RCV000206279 RCV003315718 RCV001704029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1658Gln
CA009812
NM_001354896.2:c.4973G>A