Canonical Allele Identifier: PA1139741839
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927546
ClinVar RCV Id: RCV001190913 RCV002560964 RCV003538595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2578Gln
CA048947
NM_001354896.2:c.7733G>A