Canonical Allele Identifier: PA2828003721
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142457
ClinVar RCV Id: RCV000131588 RCV000210106 RCV000211929 RCV000234415 RCV000590651 RCV002228664 RCV003998109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly2136Cys
CA012371
NM_001354902.2:c.6406G>T