Canonical Allele Identifier: PA2828047000
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187494
ClinVar RCV Id: RCV000167228 RCV003650438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2251Ser
CA012867
NM_001354904.2:c.6752A>G