Canonical Allele Identifier: PA156898
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41509
ClinVar RCV Id: RCV000034394 RCV000115109 RCV000120051 RCV000709878 RCV000757929 RCV000987552 RCV001156934 RCV003534317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gln213Glu
CA010884
NM_001127511.3:c.637C>G