Canonical Allele Identifier: PA2827976289
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469929
ClinVar RCV Id: RCV000582171 RCV003483665 RCV003651970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His1182Leu
CA035977
NM_001354899.2:c.3545A>T