Canonical Allele Identifier: PA645404058
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_001029.1:p.Gly520Ala
CA6405774
NM_001038.6:c.1559G>C