Canonical Allele Identifier: PA107793
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9377
ClinVar RCV Id: RCV000009974 RCV000009972 RCV000009973 RCV000058773 RCV000208193 RCV000183117 RCV000245905 RCV000588022 RCV000824758 RCV004545722 RCV003591625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1784Lys
CA019148
NM_198056.3:c.5350G>A