Canonical Allele Identifier: PA645402055
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411542
ClinVar RCV Id: RCV003651892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu2401Val
CA16037014
NM_001127510.3:c.7201C>G