Canonical Allele Identifier: PA297862
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135709
ClinVar RCV Id: RCV000122787 RCV000159562 RCV000210078 RCV000210900 RCV000764567 RCV000211923 RCV000656747 RCV001155575 RCV003398739 RCV003534359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1934Leu
CA010706
NM_001127510.3:c.5801C>T