Canonical Allele Identifier: PA1139677972
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 921338
ClinVar RCV Id: RCV001180690 RCV003537498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp998Asn
CA16028000
NM_001127511.3:c.2992G>A