Canonical Allele Identifier: PA2827999219
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761528
ClinVar RCV Id: RCV002419101 RCV003744014 RCV004005761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile2607Asn
CA16038702
NM_001354901.2:c.7820T>A