Canonical Allele Identifier: PA2828020702
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133
ClinVar RCV Id: RCV000165668 RCV000689521 RCV003534447 RCV003995444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile1021Val
CA008754
NM_001354906.2:c.3061A>G