Canonical Allele Identifier: PA2827977060
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_001341828.1:p.Gln1416His
CA038623
NM_001354899.2:c.4248A>C
CA16030825
NM_001354899.2:c.4248A>T