Canonical Allele Identifier: PA191047
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185103
ClinVar RCV Id: RCV000164466 RCV000206414 RCV000483817 RCV000779706 RCV003316023 RCV003995344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1947Ala
CA010734
NM_001127510.3:c.5839A>G