Canonical Allele Identifier: PA16039981
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_000029.2:p.Ile1579Phe
CA10584253
NM_000038.6:c.4735A>T