Canonical Allele Identifier: PA2827998837
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411452
ClinVar RCV Id: RCV000679085 RCV001190633 RCV002230537 RCV004001949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His2492Leu
CA16037955
NM_001354901.2:c.7475A>T