Canonical Allele Identifier: PA2828029774
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629969
ClinVar RCV Id: RCV000774833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly2576Cys
CA16038769
NM_001354903.2:c.7726G>T