Canonical Allele Identifier: PA645399729
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418012
ClinVar RCV Id: RCV000564208 RCV000732064 RCV003535743 RCV004002236 RCV002525751 RCV003962331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1254Val
CA036589
NM_001127510.3:c.3760A>G