Canonical Allele Identifier: PA2827990164
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1025683
ClinVar RCV Id: RCV002546156 RCV004005129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2628Ser
CA16038723
NM_001354900.2:c.7882C>T