Canonical Allele Identifier: PA916042387
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 427929
ClinVar RCV Id: RCV000491472 RCV000775971 RCV002231614 RCV003483636 RCV004003434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly83Glu
CA16022027
NM_001354904.2:c.248G>A