Canonical Allele Identifier: PA2825629605
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2734199
ClinVar RCV Id: RCV003535146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1010Cys
CA16027956
NM_001127510.3:c.3028A>T