Allele Registry

Canonical Allele Identifier: PA111198

Gene: CRYGD HGNC NCBI

ClinVar RCV:

RCV000018451

ClinVar Variation:

16942

HGVS (amino-acid)	Matching Registered Transcripts
NP_008822.2:p.Pro24Ser	CA214966 NM_006891.4:c.70C>T