Allele Registry

Canonical Allele Identifier: PA093518

Gene: SCNN1B HGNC NCBI

ClinVar RCV:

RCV000009388

RCV000393349

ClinVar Variation:

8840

HGVS (amino-acid)	Matching Registered Transcripts
NP_000327.2:p.Gly294Ser	CA119965 NM_000336.3:c.880G>A