Canonical Allele Identifier: PA658681779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469795
ClinVar RCV Id: RCV003537039
ClinVar Variation Id: 1371388
ClinVar RCV Id: RCV003772618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly23Arg
CA124925142
NM_001127511.3:c.67G>A
CA360611835
NM_001127511.3:c.67G>C