Canonical Allele Identifier: PA645489868
Gene: SCNN1G HGNC NCBI

Linked Data

ClinVar Variation Id: 318355
ClinVar RCV Id: RCV000274328 RCV000366583 RCV001329526 RCV002495002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030.2:p.His396Arg
CA7959806
NM_001039.4:c.1187A>G