Canonical Allele Identifier: PA2827968894
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_001341827.1:p.Gln1724His
CA16032805
NM_001354898.2:c.5172G>C
CA16032806
NM_001354898.2:c.5172G>T