Canonical Allele Identifier: PA915985714
Gene: SCNN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 9267
ClinVar RCV Id: RCV000009849 RCV003162223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153048.1:p.Ser621Leu
CA120272
NM_001159576.2:c.1862C>T