Canonical Allele Identifier: PA2825021501
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587019
ClinVar RCV Id: RCV003341980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser1737Asn
CA16032719
NM_000038.6:c.5210G>A