Canonical Allele Identifier: PA2827986832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1988396
ClinVar RCV Id: RCV003776978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1614Pro
CA16032197
NM_001354900.2:c.4840A>C