Canonical Allele Identifier: PA210561
Gene: CRYGC HGNC NCBI

Linked Data

ClinVar Variation Id: 16945
ClinVar RCV Id: RCV000018454 RCV001313043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066269.1:p.Arg168Trp
CA210560
NM_020989.4:c.502C>T