Canonical Allele Identifier: PA2828006701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 246402
ClinVar RCV Id: RCV000235893 RCV002338775 RCV003535664 RCV003998926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1419Phe
CA10584253
NM_001354905.2:c.4255A>T