Canonical Allele Identifier: PA2828020997
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140890
ClinVar RCV Id: RCV000129128 RCV000483615 RCV000646425 RCV001704052 RCV003997481 RCV003153412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1069Ala
CA008875
NM_001354906.2:c.3206T>C