Canonical Allele Identifier: PA2827996001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411520
ClinVar RCV Id: RCV000480116 RCV001186460 RCV003651884 RCV004001972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1632Leu
CA16032423
NM_001354901.2:c.4895C>T