Canonical Allele Identifier: PA2827964568
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785
ClinVar RCV Id: RCV000159530 RCV000227001 RCV000779739 RCV000568544 RCV002484993 RCV003315945 RCV003998402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg389His
CA004108
NM_001354898.2:c.1166G>A