Canonical Allele Identifier: PA2827989892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41537
ClinVar RCV Id: RCV000034422 RCV000570424 RCV002482949 RCV002513339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2545Ile
CA014009
NM_001354900.2:c.7634G>T