Allele Registry

Canonical Allele Identifier: PA1139679666

Gene: SCNN1G HGNC NCBI

ClinVar RCV:

RCV001116637

RCV001116638

ClinVar Variation:

885190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001030.2:p.Glu197Gln	CA395094964 NM_001039.4:c.589G>C