Canonical Allele Identifier: PA2828041847
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717783
ClinVar RCV Id: RCV003743871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly1520Arg
CA16032141
NM_001354904.2:c.4558G>A
CA16032142
NM_001354904.2:c.4558G>C