Allele Registry

Canonical Allele Identifier: PA130673

Gene: GNAL HGNC NCBI

ClinVar RCV:

RCV000033103

ClinVar Variation:

39969

HGVS (amino-acid)	Matching Registered Transcripts
NP_892023.1:p.Glu232Lys	CA130672 NM_182978.4:c.694G>A