Canonical Allele Identifier: PA2825020664
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230530
ClinVar RCV Id: RCV004520681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln1529Leu
CA16031374
NM_000038.6:c.4586A>T