Allele Registry

Canonical Allele Identifier: PA120277

Gene: SCNN1A HGNC NCBI

ClinVar RCV:

RCV000009852

ClinVar Variation:

9270

HGVS (amino-acid)	Matching Registered Transcripts
NP_001029.1:p.Arg81Cys	CA120276 NM_001038.6:c.241C>T