Canonical Allele Identifier: PA658659476
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485094
ClinVar RCV Id: RCV000574291 RCV002530325 RCV003537180 RCV003153743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg845Cys
CA16026883
NM_001127510.3:c.2533C>T