Canonical Allele Identifier: PA188891
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41508
ClinVar RCV Id: RCV000034392 RCV000119236 RCV000163663 RCV001151699 RCV003996156 RCV003650355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg1742His
CA009940
NM_001127510.3:c.5225G>A