Canonical Allele Identifier: PA183734
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67772
ClinVar RCV Id: RCV000058543 RCV000155885 RCV000766795 RCV001145177 RCV001145178 RCV001149459 RCV001145176 RCV000987213 RCV001149460 RCV001842325 RCV002433565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Cys1004Arg
CA016748
NM_198056.3:c.3010T>C