Canonical Allele Identifier: PA2828004138
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927392
ClinVar RCV Id: RCV001190627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2427Ser
CA048409
NM_001354902.2:c.7280A>G