Canonical Allele Identifier: PA2825021664
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629118
ClinVar RCV Id: RCV000773807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1778Thr
CA16032987
NM_000038.6:c.5332C>A