Canonical Allele Identifier: PA2828019032
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727503
ClinVar RCV Id: RCV002325843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser749Leu
CA16028114
NM_001354906.2:c.2246C>T