Canonical Allele Identifier: PA2828048522
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1476541
ClinVar RCV Id: RCV003773114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys2459Arg
CA16038172
NM_001354904.2:c.7376A>G