Canonical Allele Identifier: PA093528
Gene: SCNN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 8832
ClinVar RCV Id: RCV001120417 RCV001120139 RCV002310627 RCV000009380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000327.2:p.Gly37Ser
CA119959
NM_000336.3:c.109G>A