Canonical Allele Identifier: PA645404003
Gene: SCNN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 310148
ClinVar RCV Id: RCV000330908 RCV000387793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001029.1:p.Gly276Cys
CA6406100
NM_001038.6:c.826G>T