Canonical Allele Identifier: PA2827993137
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232924
ClinVar RCV Id: RCV000220641 RCV000485918 RCV000764563 RCV001174911 RCV002515684 RCV003743667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Tyr766Cys
CA032224
NM_001354901.2:c.2297A>G