Canonical Allele Identifier: PA2827990347
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135723
ClinVar RCV Id: RCV000218426 RCV000479454 RCV003997389 RCV003474735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg2680His
CA014419
NM_001354900.2:c.8039G>A