Canonical Allele Identifier: PA2828007142
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1446639
ClinVar RCV Id: RCV003653542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1488Leu
CA16032157
NM_001354905.2:c.4463C>T