Canonical Allele Identifier: PA2827996800
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411367
ClinVar RCV Id: RCV000457967 RCV000561037 RCV000679070 RCV004001924
ClinVar Variation Id: 630647
ClinVar RCV Id: RCV000776593 RCV003744648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1873Ser
CA043023
NM_001354901.2:c.5617A>T
CA16034011
NM_001354901.2:c.5618C>G