Canonical Allele Identifier: PA2828014514
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418609
ClinVar RCV Id: RCV000482238 RCV000570748 RCV002525774 RCV004002259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Leu21Pro
CA16023306
NM_001354906.2:c.62T>C