Canonical Allele Identifier: PA2829198256
Gene: CRACD HGNC NCBI

Linked Data

ClinVar Variation Id: 3077091
ClinVar RCV Id: RCV004374867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380310.1:p.Gln571Arg
CA356980189
NM_001393381.1:c.1712A>G