Canonical Allele Identifier: PA2741927476
Gene: CRYGD HGNC NCBI

Linked Data

ClinVar Variation Id: 2633209
ClinVar RCV Id: RCV003399977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008822.2:p.Cys79Tyr
CA350092484
NM_006891.4:c.236G>A