Canonical Allele Identifier: PA645396650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 420793
ClinVar RCV Id: RCV000484135 RCV000574492 RCV000766533 RCV000646444 RCV002282167 RCV003651926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg98Trp
CA032840
NM_001127511.3:c.292C>T