Canonical Allele Identifier: PA2825015020
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 961490
ClinVar RCV Id: RCV001235188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val450Ala
CA16024258
NM_000038.6:c.1349T>C