Canonical Allele Identifier: PA286671
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127317
ClinVar RCV Id: RCV000115119 RCV001026018 RCV003534344 RCV003997229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys2363Arg
CA012825
NM_001127510.3:c.7088A>G