Canonical Allele Identifier: PA107875
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9395
ClinVar RCV Id: RCV000009995 RCV000009996 RCV000009997 RCV000058649 RCV000183190 RCV002326672 RCV002496318 RCV003996085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly1408Arg
CA017985
NM_198056.3:c.4222G>A
CA352146220
NM_198056.3:c.4222G>C