Canonical Allele Identifier: PA645400055
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411562
ClinVar RCV Id: RCV000571742 RCV001550235 RCV002526464 RCV002489079 RCV003535737 RCV004001983
ClinVar Variation Id: 941479
ClinVar RCV Id: RCV002327487 RCV003650695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln1444His
CA038623
NM_001127510.3:c.4332A>C
CA16030825
NM_001127510.3:c.4332A>T