Canonical Allele Identifier: PA2827998825
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759946
ClinVar RCV Id: RCV002396364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Trp2488Cys
CA16037928
NM_001354901.2:c.7464G>C
CA16037929
NM_001354901.2:c.7464G>T