Canonical Allele Identifier: PA2827956972
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485127
ClinVar RCV Id: RCV000570077 RCV001584390 RCV002528960 RCV003537188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His923Arg
CA033216
NM_001354897.2:c.2768A>G