Canonical Allele Identifier: PA2827959759
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486737
ClinVar RCV Id: RCV000561457 RCV002232177 RCV003126826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln1759His
CA16032805
NM_001354897.2:c.5277G>C
CA16032806
NM_001354897.2:c.5277G>T