Canonical Allele Identifier: PA2827989862
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 922223
ClinVar RCV Id: RCV001182155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2536Pro
CA16038115
NM_001354900.2:c.7606T>C