Canonical Allele Identifier: PA2828021181
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233890
ClinVar RCV Id: RCV000223239 RCV000522947 RCV003743680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr1097Ile
CA10578369
NM_001354906.2:c.3290C>T