Allele Registry

Canonical Allele Identifier: PA104528

Gene: GNAL HGNC NCBI

ClinVar RCV:

RCV000033103

ClinVar Variation:

39969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135811.1:p.Glu155Lys	CA130672 NM_001142339.3:c.463G>A