Canonical Allele Identifier: PA2827980701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216179
ClinVar RCV Id: RCV002269262 RCV001185305 RCV002291592 RCV003993886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2525Gln
CA338557
NM_001354899.2:c.7573A>C