Canonical Allele Identifier: PA2825020702
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2105453
ClinVar RCV Id: RCV003744909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1537Pro
CA3368168
NM_000038.6:c.4609A>C