Canonical Allele Identifier: PA2827953291
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760034
ClinVar RCV Id: RCV002396452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His2572Asn
CA16037972
NM_001354896.2:c.7714C>A