Allele Registry

Canonical Allele Identifier: PA111205

Gene: CRYGD HGNC NCBI

ClinVar RCV:

RCV000018448

RCV000203330

RCV001061709

RCV001596934

ClinVar Variation:

16940

HGVS (amino-acid)	Matching Registered Transcripts
NP_008822.2:p.Pro24Thr	CA214963 NM_006891.4:c.70C>A