Canonical Allele Identifier: PA2827977816
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127302
ClinVar RCV Id: RCV000120016 RCV000115100 RCV000210376 RCV000587987 RCV000735965 RCV001353642 RCV003323290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg1648Gly
CA009838
NM_001354899.2:c.4942A>G
CA2740097766
NM_001354899.2:c.4942_4950delinsGGAGGAGGA