Canonical Allele Identifier: PA2829198217
Gene: CRACD HGNC NCBI

Linked Data

ClinVar Variation Id: 2558143
ClinVar RCV Id: RCV004329401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380310.1:p.Thr3Ala
CA2928436
NM_001393381.1:c.7A>G