Canonical Allele Identifier: PA2827987228
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1332383
ClinVar RCV Id: RCV001805429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1732Pro
CA16032957
NM_001354900.2:c.5194A>C