Canonical Allele Identifier: PA2828002513
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2775064
ClinVar RCV Id: RCV003585112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu1484Arg
CA16031693
NM_001354902.2:c.4451T>G