Canonical Allele Identifier: PA2827982957
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1770469
ClinVar RCV Id: RCV002387817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala390Ser
CA16024250
NM_001354900.2:c.1168G>T