Canonical Allele Identifier: PA156828
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526
ClinVar RCV Id: RCV000120036 RCV003743574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1018Asn
CA008010
NM_001127510.3:c.3052G>A