Canonical Allele Identifier: PA2827971882
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2914999
ClinVar RCV Id: RCV003652941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2635Ile
CA049562
NM_001354898.2:c.7904G>T