Canonical Allele Identifier: PA2573255519
Gene: CRYGD HGNC NCBI

Linked Data

ClinVar Variation Id: 1358725
ClinVar RCV Id: RCV001872079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008822.2:p.Cys33Arg
CA350092783
NM_006891.4:c.97T>C