Allele Registry

Canonical Allele Identifier: PA2828323746

Gene: GNAL HGNC NCBI

ClinVar RCV:

RCV000033101

RCV003236771

ClinVar Variation:

39967

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356316.1:p.Val137Met	CA130667 NM_001369387.1:c.409G>A