Canonical Allele Identifier: PA916039918
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135690
ClinVar RCV Id: RCV000122764 RCV000131163 RCV000238728 RCV000348086 RCV000587302 RCV003743577 RCV002228418 RCV003492529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro883Ser
CA007632
NM_001354896.2:c.2647C>T