Canonical Allele Identifier: PA913200298
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628083
ClinVar RCV Id: RCV000772383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln1701Glu
CA16032483
NM_001127510.3:c.5101C>G