Allele Registry

Canonical Allele Identifier: PA107399

Gene: CRYGC HGNC NCBI

ClinVar RCV:

RCV000018452

RCV003593862

ClinVar Variation:

16943

HGVS (amino-acid)	Matching Registered Transcripts
NP_066269.1:p.Thr5Pro	CA126997 NM_020989.4:c.13A>C