Canonical Allele Identifier: PA297930
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181824
ClinVar RCV Id: RCV000159576 RCV000211935 RCV000656751 RCV003998423 RCV003534415 RCV002516419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg2512Trp
CA013892
NM_001127511.3:c.7534C>T