Canonical Allele Identifier: PA2828006301
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230474
ClinVar RCV Id: RCV000214073 RCV003477717 RCV003743650 RCV003997841 RCV000461981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1299Ser
CA038928
NM_001354905.2:c.3896C>G
CA16030912
NM_001354905.2:c.3895A>T