Canonical Allele Identifier: PA2827959042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482326
ClinVar RCV Id: RCV000574767 RCV000677757 RCV002232417 RCV003153739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1541His
CA16031385
NM_001354897.2:c.4621A>C