Canonical Allele Identifier: PA111167
Gene: CRYGD HGNC NCBI

Linked Data

ClinVar Variation Id: 16939
ClinVar RCV Id: RCV000018447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008822.2:p.Arg37Ser
CA214962
NM_006891.4:c.109C>A