Canonical Allele Identifier: PA297882
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181814
ClinVar RCV Id: RCV000159566 RCV000575448 RCV002265632 RCV003534413 RCV003998418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2224Val
CA012361
NM_001127510.3:c.6670A>G