Canonical Allele Identifier: PA916041486
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 664699
ClinVar RCV Id: RCV002390703 RCV004002847 RCV003537299
ClinVar Variation Id: 1759394
ClinVar RCV Id: RCV002393894
ClinVar Variation Id: 3231329
ClinVar RCV Id: RCV004525400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2530Arg
CA16037706
NM_001354896.2:c.7588A>C
CA16037712
NM_001354896.2:c.7590T>A
CA16037713
NM_001354896.2:c.7590T>G