Canonical Allele Identifier: PA2828053854
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_001341834.1:p.Leu469Ser
CA16025442
NM_001354905.2:c.1406T>C