Canonical Allele Identifier: PA645396639
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411444
ClinVar RCV Id: RCV000479660 RCV000571928 RCV001192982 RCV002506131 RCV003766575 RCV004001947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg81His
CA030877
NM_001127511.3:c.242G>A