Allele Registry

Canonical Allele Identifier: PA126995

Gene: CRYM HGNC NCBI

ClinVar RCV:

RCV000018443

ClinVar Variation:

16935

HGVS (amino-acid)	Matching Registered Transcripts
NP_001879.1:p.Lys314Thr	CA126994 NM_001888.5:c.941A>C