Canonical Allele Identifier: PA2827959096
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2167776
ClinVar RCV Id: RCV003653675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1556Ser
CA16031491
NM_001354897.2:c.4667A>G