Canonical Allele Identifier: PA915985054
Gene: CRYGD HGNC NCBI

Linked Data

ClinVar Variation Id: 657292
ClinVar RCV Id: RCV000813871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008822.2:p.His84Gln
CA2077694
NM_006891.4:c.252C>A
CA350092452
NM_006891.4:c.252C>G