Canonical Allele Identifier: PA2827992042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692142
ClinVar RCV Id: RCV002258480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val391Gly
CA027234
NM_001354901.2:c.1172T>G