Canonical Allele Identifier: PA2828028477
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128
ClinVar RCV Id: RCV002391534 RCV003475357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.His2213Gln
CA16037618
NM_001354906.2:c.6639T>A
CA16037619
NM_001354906.2:c.6639T>G