Canonical Allele Identifier: PA2828041241
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1047925
ClinVar RCV Id: RCV001352685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile1453Thr
CA16031719
NM_001354904.2:c.4358T>C