Canonical Allele Identifier: PA2828001556
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2011308
ClinVar RCV Id: RCV003742932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1022Asp
CA16028649
NM_001354902.2:c.3064A>G