Canonical Allele Identifier: PA2828019707
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629986
ClinVar RCV Id: RCV000774851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp851Gly
CA16028788
NM_001354906.2:c.2552A>G