Canonical Allele Identifier: PA297947
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827
ClinVar RCV Id: RCV000159579 RCV000583290 RCV003534416 RCV003230419 RCV002515105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2626Ile
CA014137
NM_001127510.3:c.7877C>T