Canonical Allele Identifier: PA2825020338
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469962
ClinVar RCV Id: RCV000708640 RCV001155476 RCV002526273 RCV003328596 RCV003999394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1448Ile
CA16030848
NM_000038.6:c.4343C>T