Canonical Allele Identifier: PA111205
Gene: CRYGD HGNC NCBI

Linked Data

ClinVar Variation Id: 16940
ClinVar RCV Id: RCV000018448 RCV000203330 RCV001596934 RCV001061709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008822.2:p.Pro24Thr
CA214963
NM_006891.4:c.70C>A