Canonical Allele Identifier: PA2828012639
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_001341834.1:p.Trp2387Cys
CA16037928
NM_001354905.2:c.7161G>C
CA16037929
NM_001354905.2:c.7161G>T