Canonical Allele Identifier: PA156867
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133534
ClinVar RCV Id: RCV000120044 RCV000222733 RCV003997335 RCV003650379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg2530Gln
CA013904
NM_000038.6:c.7589G>A