Canonical Allele Identifier: PA297775
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181793
ClinVar RCV Id: RCV000159539 RCV000205053 RCV000572390 RCV000779726 RCV003998408 RCV003743593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val821Ile
CA007489
NM_001127510.3:c.2461G>A