Canonical Allele Identifier: PA1139763154
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 859529
ClinVar RCV Id: RCV003656394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1999Asp
CA352139153
NM_198056.3:c.5997A>T
CA352139157
NM_198056.3:c.5997A>C