Canonical Allele Identifier: PA2828007111
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_001341834.1:p.Gly1486Arg
CA16032141
NM_001354905.2:c.4456G>A
CA16032142
NM_001354905.2:c.4456G>C