Allele Registry

Canonical Allele Identifier: PA130668

Gene: GNAL HGNC NCBI

ClinVar RCV:

RCV000033101

RCV003236771

ClinVar Variation:

39967

HGVS (amino-acid)	Matching Registered Transcripts
NP_892023.1:p.Val214Met	CA130667 NM_182978.4:c.640G>A