Canonical Allele Identifier: PA915985710
Gene: SCNN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 310134
ClinVar RCV Id: RCV000337730 RCV000400458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153048.1:p.Gly579Ala
CA6405774
NM_001159576.2:c.1736G>C