Canonical Allele Identifier: PA191282
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185193
ClinVar RCV Id: RCV000164563 RCV000239027 RCV000544500 RCV001353563 RCV002478503 RCV003534443 RCV003995351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg374Gln
CA004057
NM_001127510.3:c.1121G>A