Canonical Allele Identifier: PA916042000
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469904
ClinVar RCV Id: RCV001018532 RCV001724055 RCV002526253 RCV003537065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser987Ile
CA16028086
NM_001354900.2:c.2960G>T