Allele Registry

Canonical Allele Identifier: PA2826482718

Gene: GNAL HGNC NCBI

ClinVar RCV:

RCV000033101

RCV003236771

ClinVar Variation:

39967

HGVS (amino-acid)	Matching Registered Transcripts
NP_001248372.1:p.Val137Met	CA130667 NM_001261443.2:c.409G>A