Canonical Allele Identifier: PA2829949254
Gene: CRACD HGNC NCBI

Linked Data

ClinVar Variation Id: 3077091
ClinVar RCV Id: RCV004374867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065773.1:p.Gln571Arg
CA356980189
NM_020722.1:c.1712A>G