Canonical Allele Identifier: PA2825627460
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926362
ClinVar RCV Id: RCV001188921 RCV002560936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu629Ser
CA16025442
NM_001127510.3:c.1886T>C