Canonical Allele Identifier: PA2825131862
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3074553
ClinVar RCV Id: RCV004014087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1598Ala
CA352143603
NM_000335.5:c.4793T>C