Canonical Allele Identifier: PA658803738
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537483
ClinVar RCV Id: RCV001020071 RCV002530048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His1119Leu
CA16028686
NM_001127510.3:c.3356A>T