Canonical Allele Identifier: PA2827996176
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2567011
ClinVar RCV Id: RCV003306859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys1680Asn
CA16032735
NM_001354901.2:c.5040G>C
CA16032736
NM_001354901.2:c.5040G>T